Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
https://web.expasy.org/cellosaurus/CVCL_7268
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_7268 Copy
https://web.expasy.org/cellosaurus/CVCL_LB61
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Characteristics: The luciferase reporter gene is under the control of a minimal TATA promoter with multiple copies of the NF-kappaB response element.
Proper citation: RRID:CVCL_LB61 Copy
https://web.expasy.org/cellosaurus/CVCL_1F01
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type III
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00111, RRID:CVCL_1F01 Copy
https://web.expasy.org/cellosaurus/CVCL_7273
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM00043, RRID:CVCL_7273 Copy
https://web.expasy.org/cellosaurus/CVCL_R904
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_R904 Copy
https://web.expasy.org/cellosaurus/CVCL_X224
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00088, RRID:CVCL_X224 Copy
https://web.expasy.org/cellosaurus/CVCL_L495
Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group A
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: JCRB Cat# KURB1026, RRID:CVCL_L495 Copy
https://web.expasy.org/cellosaurus/CVCL_2N23
Organism: Homo sapiens (Human)
Disease: Propionic acidemia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00057, RRID:CVCL_2N23 Copy
https://web.expasy.org/cellosaurus/CVCL_0P14
Organism: Homo sapiens (Human)
Disease: Canavan disease
Category: Finite cell line
Proper citation: RRID:CVCL_0P14 Copy
https://web.expasy.org/cellosaurus/CVCL_V747
Organism: Homo sapiens (Human)
Disease: Simpson Golabi Behmel syndrome type 1
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;1)(q26;q21) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00097, RRID:CVCL_V747 Copy
https://web.expasy.org/cellosaurus/CVCL_F600
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;19)(q22;q13.3) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00089, RRID:CVCL_F600 Copy
https://web.expasy.org/cellosaurus/CVCL_V749
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(15)(15qter->15p1::Yq11->Yqter)pat (Coriell=GM00118)., Population: Caucasian; Danish.
Proper citation: RRID:CVCL_V749 Copy
https://web.expasy.org/cellosaurus/CVCL_9R60
Organism: Homo sapiens (Human)
Disease: Mucolipidosis type IIIA
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9R60 Copy
https://web.expasy.org/cellosaurus/CVCL_L495
Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group A
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00082, RRID:CVCL_L495 Copy
https://web.expasy.org/cellosaurus/CVCL_V459
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00144, RRID:CVCL_V459 Copy
https://web.expasy.org/cellosaurus/CVCL_4J08
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: African; Kenyan.
Proper citation: RRID:CVCL_4J08 Copy
https://web.expasy.org/cellosaurus/CVCL_X224
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_X224 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD92
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_JD92 Copy
https://web.expasy.org/cellosaurus/CVCL_H961
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;3)(q28;q21) (Coriell=GM00194)., Population: Caucasian; Finnish.
Proper citation: Coriell Cat# GM00194, RRID:CVCL_H961 Copy
https://web.expasy.org/cellosaurus/CVCL_V460
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM00201, RRID:CVCL_V460 Copy
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